Combined XPS and TPD study of oxygen-functionalized carbon nanofibers grown on sintered metal fibers

被引:193
|
作者
Rosenthal, Dirk [1 ]
Ruta, Marina [2 ]
Schloegl, Robert [1 ]
Kiwi-Minsker, Lioubov [2 ]
机构
[1] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[2] Ecole Polytech Fed Lausanne, GGRC EPFL, Stn 6, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
CONTAINING SURFACE GROUPS; ACTIVATED CARBONS; NANOTUBES; OXIDATION; HYDROGENATION; CHEMISTRY; POLYMERS; CATALYST; SPECTRA; FILTERS;
D O I
10.1016/j.carbon.2010.01.029
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A composite material consisting of carbon nanofibers (CNFs) grown on sintered metal fiber filters was modified by H(2)O(2) or plasma-generated O(3). Coupling temperature programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS) techniques in the same UHV apparatus allowed the direct correlation of the nature of the created O-functional groups and their evolution as CO and CO(2) upon heating. The two oxidative treatments yielded different distributions of O-containing groups. The relative contribution of oxidized carbon was very low in the C1s region, hence the functional groups were more robustly analyzed through the O1s region. The comparison of the released oxygen by integration of the TPD CO, CO(2) and H(2)O spectra with the intensity loss of the XPS O1s spectra showed good agreement. In order to fit the data adequately, the set of O1s spectra was deconvoluted in at least four peaks for the differently activated samples. Finally, it was shown that functional groups formed by H(2)O(2)-treatment (mostly non-phenolic OH groups) are more thermally stable than those formed by O(3)-treatment. The latter treatment increases the concentration of carboxylic functionalities, which decompose at temperatures < 800 K; O(3)-activated CNFs should therefore show a more pronounced acidic behavior. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1835 / 1843
页数:9
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